Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010806878

FEI Number

3010806878

Entity Name

QX WORLD KFT

City/State/Country

Budapest, HU

Establishment Address

Tinodi utca 1-3, A. ep. IV. em. 93, Budapest 1095, HU

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

QX World KFT (Owner Number: 10054119)

Owner / Operator Contact Address

Tinodi utca 1-3, A.ep. IV. em. 93, Budapest, HU-BU 1095, HU

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K232779

PMA Number

N/A

All Registered Proprietary Names

QUEX ED QUEX S

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OMC	Reduced- Montage Standard Electroencephalograph	Neurology	Class 2	882.1400	2025-07-03
GZO	Device, Galvanic Skin Response Measurement	Neurology	Class 2	882.1540	2025-07-03

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

QX World KFT

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010806878. Last updated year: 2026. Please use registration number 3010806878 when referencing this establishment in official correspondence.